Reporting of Suspected Adverse Drug Reactions for Human Use: Pharmacovigilance

At Pharmaceutical Innovation Services S.L., we are committed to ensuring the safety of the medicines we commercialize. As the holder of the marketing authorization for medicines, we are obligated to maintain a surveillance system that allows us to manage suspected adverse drug reactions (ADRs) for human use.

If you are aware of any suspected adverse drug reaction for human use related to one of our products, please report it using one of the following methods:

1. Reporting form: Please fill out the form located on the left-hand side to submit any adverse reaction.
2. Phone (24 hours): Call us at 644 13 55 02 / 655 30 63 03 to report any adverse event directly.
3. Email: You can also send your report to pv@, and our pharmacovigilance team will handle your case.

Pharmacovigilance is the science and activities relating to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. At Pharmaceutical Innovation Services S.L., we carry out monitoring and surveillance activities, which include reviewing and evaluating reports of suspected adverse reactions, epidemiological studies, published literature, and/or additional clinical trials.

Our goal is to guarantee the highest level of safety for the products we distribute. Therefore, it is essential that any potential adverse event is reported through our official channels.

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